Imatinib increases apoptosis index through modulation of survivin subcellular localization in the blast phase of CML cells

被引:11
作者
Bernardo, Paula Sabbo [1 ]
de Souza Reis, Flaviana Ruade [1 ]
Maia, Raquel Ciuvalschi [1 ]
机构
[1] Inst Nacl Canc INCA, Lab Hematooncol Celular & Mol, Programa Pesquisa Hematooncol Mol, Rio De Janeiro, RJ, Brazil
关键词
Chronic myeloid leukemia; Survivin; P-glycoprotein; Imatinib; Subcellular localization; CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; TYROSINE KINASE INHIBITOR; P-GLYCOPROTEIN; MULTIDRUG-RESISTANCE; SPLICE VARIANTS; BREAST-CANCER; PROGNOSTIC-SIGNIFICANCE; CYTOPLASMIC EXPRESSION; ANTILEUKEMIC AGENTS;
D O I
10.1016/j.leukres.2012.08.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using MTT, Annexin V/flow cytometry, immunocytochemistry, subcellular fractionation, and Western blotting assays we analyzed the effect of imatinib in two blast phase of chronic myeloid leukemia (CML) cell lines: K562 P-glycoprotein (Pgp)-negative, and Lucena, Pgp-positive. In K562 cell line, the high apoptosis index induced by imatinib was associated with the survivin predominantly in the nucleus. In the Lucena cell line, the low apoptosis index induced by imatinib was associated with a cytoplasmatic survivin localization. Pgp and survivin might be subject to the same molecular regulation, and therefore represent a therapeutic target in the blast phase of CML. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1510 / 1516
页数:7
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